Regulatory Affairs Consultant - Head - GO/JC/1061/2025

Minimum of 10 years of Life Science industry experience, with substantial exposure to regulatory affairs.Hands on experience and demonstrated expertise in Chemistry, Manufacturing, and labeling processingComprehensive understanding of global regulatory framework, including FDA, EMA, ICH and other international standards.Excellent communication skills both written and verbalMeticulous attention to detail and organizational prowessProficiency in project management and cross-functional collaborationStrong analytical and problem-solving skillsAbility to navigate and interpret complex regulatory landscapes across multiple regionsGood understanding of Quality Management Systems in the outsourcing scenariosMust have skill setCMClabeling processglobal regulatory frameworksGood Clinical PracticeQuality ManagementFDAEMAICH

Skills Required

RoleRegulatory Affairs Consultant - HeadIndustry TypePharmaceuticalsFunctional AreaRequired Education BachelorEmployment TypeFull Time, PermanentKey Skills

• CMC
• LABELING
• GOOD CLINICAL PRACTICE
• FDA
  

Other Information
Job CodeGO/JC/1061/2025Recruiter NameMaheshwari Balasubramanian